# K220244: DVR® Crosslock Wrist Spanning Plate (131849181)

- Pathway: 510(k) (Traditional)
- Applicant: Pioneer Surgical Technology, Inc D.B.A Resolve Surgical Tech
- Decided: Apr 28, 2022 after 90 days
- Product code: HRS (Plate, Fixation, Bone)
- Device class: 2
- Regulation: 21 CFR 888.3030
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 10 generations back to K000684 (2000). 51 ancestors in all.
No later device cites it as a predicate yet.
0 of 52 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K143749: Arthrex Distal Radius System, Arthrex, Inc. (2015)

## Indications for use
The DVR® Crosslock Wrist Spanning Plate is indicated for skeletally mature patients for fixation of fractures, osteotomies and non-unions of the distal radius.

Source page: https://510kreport.com/device/K220244
Methodology: https://510kreport.com/methodology